Analyze Diet

Whole-genome scan identifies quantitative trait loci for chronic pastern dermatitis in German draft horses.

Abstract: Chronic pastern dermatitis (CPD), also known as chronic progressive lymphedema (CPL), is a skin disease that affects draft horses. This disease causes painful lower-leg swelling, nodule formation, and skin ulceration, interfering with movement. The aim of this whole-genome scan was to identify quantitative trait loci (QTL) for CPD in German draft horses. We recorded clinical data for CPD in 917 German draft horses and collected blood samples from these horses. Of these 917 horses, 31 paternal half-sib families comprising 378 horses from the breeds Rhenish German, Schleswig, Saxon-Thuringian, and South German were chosen for genotyping. Each half-sib family was constituted by only one draft horse breed. Genotyping was done for 318 polymorphic microsatellites evenly distributed on all equine autosomes and the X chromosome with a mean distance of 7.5 Mb. An across-breed multipoint linkage analysis revealed chromosome-wide significant QTL on horse chromosomes (ECA) 1, 9, 16, and 17. Analyses by breed confirmed the QTL on ECA1 in South German and the QTL on ECA9, 16, and 17 in Saxon-Thuringian draft horses. For the Rhenish German and Schleswig draft horses, additional QTL on ECA4 and 10 and for the South German draft horses an additional QTL on ECA7 were found. This is the first whole-genome scan for CPD in draft horses and it is an important step toward the identification of candidate genes.
Publication Date: 2009-12-29 PubMed ID: 20039044DOI: 10.1007/s00335-009-9244-zGoogle Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This research studied a skin disease in German draft horses, named chronic pastern dermatitis (CPD), and identified specific chromosomes in the horse genome that influence the occurrence of the disease. Through sampling and genotyping various draft horse breeds, the researchers found significant quantitative trait loci (QTL) on four specific chromosomes.

Chronic Pastern Dermatitis (CPD) and Objective of the Study

  • This research investigates Chronic Pastern Dermatitis (CPD), a harmful skin disease that causes painful swelling, skin ulceration, and nodule formation in the lower legs of draft horses, affecting their ability to move.
  • The purpose of the whole-genome scan was to discover if certain locations in the genome (quantitative trait loci or QTL) are associated with CPD in German draft horses.

Methodology

  • For the research, clinical data of CPD were recorded from 917 German draft horses and blood samples were collected from them.
  • From the total sample size, 31 paternal half-sib families—an aggregation of siblings that share the same father—were chosen. These families comprised of 378 horses hailing from four different German draft horse breeds.
  • The genotyping was done on 318 polymorphic microsatellites—bits of DNA that are assessed for genetic differences—across the equine autosomes (non-sex chromosomes) and the X chromosome.

Findings

  • Through multipoint linkage analysis—a statistical method used to find out which genes are inherited together—the researchers found significant QTL for CPD on four horse chromosomes (ECA 1, 9, 16, and 17).
  • The QTL on ECA1 was confirmed in South German draft horses, and those on ECA9, 16, and 17 in Saxon-Thuringian draft horses.
  • Rhenish German and Schleswig draft horses had additional QTL on ECA4 and 10, and for the South German draft horses, an additional QTL on ECA7 was located.

Importance and Implications of the Research

  • This study is the first whole-genome scan for CPD in draft horses, hence it paves the way for future research. The identification of these QTLs is crucial as it can lead to the discovery of candidate genes that cause CPD.
  • Understanding the genetic factors contributing to CPD can help in developing prevention strategies and treatments for this disease, improving the well-being and quality of life of draft horses.

Cite This Article

APA
Mittmann EH, Mömke S, Distl O. (2009). Whole-genome scan identifies quantitative trait loci for chronic pastern dermatitis in German draft horses. Mamm Genome, 21(1-2), 95-103. https://doi.org/10.1007/s00335-009-9244-z

Publication

ISSN: 1432-1777
NlmUniqueID: 9100916
Country: United States
Language: English
Volume: 21
Issue: 1-2
Pages: 95-103

Researcher Affiliations

Mittmann, E Henrike
  • Institute of Animal Breeding and Genetics, University of Veterinary Medicine Hannover, Bünteweg 17p, 30559, Hannover, Germany.
Mömke, Stefanie
    Distl, Ottmar

      MeSH Terms

      • Animals
      • Chromosomes, Mammalian / genetics
      • Chronic Disease
      • Dermatitis / genetics
      • Dermatitis / veterinary
      • Foot Diseases / genetics
      • Foot Diseases / veterinary
      • Genome-Wide Association Study
      • Genotype
      • Horse Diseases / genetics
      • Horses / genetics
      • Lod Score
      • Lymphedema / genetics
      • Lymphedema / veterinary
      • Microsatellite Repeats
      • Quantitative Trait Loci

      References

      This article includes 22 references
      1. J Cell Biochem. 2009 Apr 15;106(6):1123-35
        pubmed: 19204938
      2. Mol Cell Biol. 2006 Aug;26(15):5595-602
        pubmed: 16847315
      3. Biometrics. 1994 Mar;50(1):118-27
        pubmed: 8086596
      4. Am J Hum Genet. 1997 Nov;61(5):1179-88
        pubmed: 9345087
      5. Vet J. 2007 Sep;174(2):397-9
        pubmed: 16884936
      6. Lymphat Res Biol. 2003;1(3):191-9
        pubmed: 15624437
      7. Anim Genet. 2004 Aug;35(4):270-7
        pubmed: 15265065
      8. Genome Res. 2003 Apr;13(4):742-51
        pubmed: 12671008
      9. Am J Hum Genet. 1996 Jun;58(6):1347-63
        pubmed: 8651312
      10. Vet Dermatol. 2005 Dec;16(6):373-84
        pubmed: 16359304
      11. Anim Genet. 2010 Apr;41(2):222
        pubmed: 19793266
      12. Lymphat Res Biol. 2006;4(2):67-72
        pubmed: 16808668
      13. FASEB J. 2006 Jul;20(9):1525-7
        pubmed: 16754747
      14. Bioinformatics. 2005 Aug 15;21(16):3445-7
        pubmed: 15947021
      15. Nat Genet. 2002 Jan;30(1):97-101
        pubmed: 11731797
      16. Cytogenet Genome Res. 2008;122(1):28-36
        pubmed: 18931483
      17. Berl Munch Tierarztl Wochenschr. 2004 Jan-Feb;117(1-2):72-5
        pubmed: 14964127
      18. Cytogenet Genome Res. 2007;116(4):256-62
        pubmed: 17431323
      19. Genomics. 2006 Jan;87(1):1-29
        pubmed: 16314071
      20. Berl Munch Tierarztl Wochenschr. 2004 Mar-Apr;117(3-4):148-52
        pubmed: 15046463
      21. J Hered. 2007 May-Jun;98(3):267-71
        pubmed: 17395600
      22. Cytogenet Genome Res. 2005;111(1):5-15
        pubmed: 16093715